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Variant : CV602044 (GRCh37/hg19 8p23.1(chr8:7191245-8165004)x1) Homo sapiens

Symbol: CV602044
Name: GRCh37/hg19 8p23.1(chr8:7191245-8165004)x1
Condition: not provided [RCV000747344]
Clinical Significance: benign
Last Evaluated: 11/02/2010
Review Status: no assertion criteria provided
Related Genes: DEFB103A   DEFB103B   DEFB104A   DEFB104B   DEFB105A   DEFB105B   DEFB106A   DEFB106B   DEFB107A   DEFB107B   DEFB4A   DEFB4B   SPAG11A   SPAG11B   USP17L1   USP17L3   USP17L4   USP17L8   ZNF705B   ZNF705G  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3787,191,245 - 8,165,004CLINVAR
Cytogenetic Map88p23.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14362689
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-07-07
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.